Highly Regioselective Hydroaminomethylation for Amine Synthesis Enabled by a Heterogeneous Molecular Catalyst Ru <sub>3</sub> /QDPOP

In this work, we report an efficient protocol for direct amine synthesis from alkenes catalyzed by a heterogeneous molecular catalyst Ru<sub>3</sub>/QDPOP, which features well-defined trinuclear Rh centers stabilized by a phosphine-functionalized porous organic polymer. The catalyst exhibited high activity and excellent regioselectivity toward the desired linear amines, significantly surpassing previously reported homo- and heterogeneous Ru-based catalysts. Various secondary and tertiary amines, including pharmaceutically relevant compounds, can be effectively synthesized from diverse amines and alkenes under mild conditions. Moreover, the catalyst is stable and recyclable, maintaining high performance over five cycles without appreciable loss in performance.

Authors

Institutions

Publication Details

Journal
Organic Letters
Published
2026-02-01
DOI
https://doi.org/10.1021/acs.orglett.5c05238
Primary Topic
Asymmetric Hydrogenation and Catalysis
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Highly Regioselective Hydroaminomethylation for Amine Synthesis Enabled by a Heterogeneous Molecular Catalyst Ru 3 /QDPOP

Yinghao Zhu, Yong Yang, Bhalchandra M. Bhanage, Zhaozhan Wang et al.
Organic Letters
Asymmetric Hydrogenation and Catalysis
article

Highly Regioselective Hydroaminomethylation for Amine Synthesis Enabled by a Heterogeneous Molecular Catalyst Ru 3 /QDPOP

Yinghao Zhu, Yong Yang, Bhalchandra M. Bhanage, Zhaozhan Wang, Chen Li
article en

Abstract

In this work, we report an efficient protocol for direct amine synthesis from alkenes catalyzed by a heterogeneous molecular catalyst Ru<sub>3</sub>/QDPOP, which features well-defined trinuclear Rh centers stabilized by a phosphine-functionalized porous organic polymer. The catalyst exhibited high activity and excellent regioselectivity toward the desired linear amines, significantly surpassing previously reported homo- and heterogeneous Ru-based catalysts. Various secondary and tertiary amines, including pharmaceutically relevant compounds, can be effectively synthesized from diverse amines and alkenes under mild conditions. Moreover, the catalyst is stable and recyclable, maintaining high performance over five cycles without appreciable loss in performance.

Organic LettersVol. 28(6)
Energy Institute (GB), Institute of Chemical Technology (IN), Chinese Academy of Sciences (CN), Tianjin Municipal Engineering Design and Research Institute (CN), Shandong Lianxing Energy Group (China) (CN), Qingdao Institute of Bioenergy and Bioprocess Technology (CN), University of Chinese Academy of Sciences (CN)
Openalex Percentile: Top 71%
Asymmetric Hydrogenation and Catalysis
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.